Page 12 - Morphoanatomical investigations of cones and pollen in Cathaya argyrophylla Chung & Kuang (Pinaceae, Coniferales) under systematical and evolutional aspects
P. 12

V. M. Dörken and H. Nimsch                                        Feddes Repertorium 2014, 125, 25–38

            res as occuring e.g. in  Taxus  (Taxaceae) as derived   lous microsporangiophores the central sporangia hardly
            from a radial synangium consisting of several dorsiven-  can be inserted lateral at the margin of a sporophyll.
            tral reduced sporangiophores. Apart from normal micro-  Among conifers the evolution of a dorsiventral bauplan
            sporangiophores with two microsporangia the investi-  of microsporangiophores might represent an optimiza-
            gated  Cathaya pollen-cones showed also micro-     tion in respect to several  functional aspects such as
            sporangiophores with three sporangia. This is also    protection of sporangia before anthesis and secondary
            described for  Picea asperata where sometimes micro-  pollen exposition, both also realized in  Cathaya. Fur-
            sporangiophores with three or four sporangia have been   thermore the dorsiventral bauplan allows a more dense
            found (Mundry 2000). Such anomalies may lead to the   arrangement of sporangiophores at the cone axis, than it
            idea that microsporangiophores in Pinaceae represent a   would be possible in perisporangiate cones (Mundry
            reduced structure derived from a perisporangiate spo-  2000).
            rangiophore as it could be shown for  Torreya (Tax-
            aceae). In studies on the character state evolution of   We are grateful to Dr. Michael  Laumann and Mrs.
            Taxaceae pollen-cones (e.g. Wilde 1975; Mundry &   Lauretta  Nejedli  (Electron Microscopy Center, Depart-
            Mundry 2001; Dörken et al. 2011) a complete transition   ment of Biology, University of Konstanz, Germany) for
            line beginning with inflorescence-like cones in Cephalo-  technical support (SEM and paraffin technique). Fur-
            taxus and ending with flower-like cones in  Taxus and   thermore we thank Mr. Oliver St. John (Sheffield, Eng-
            Torreya  could be shown. Pollen-cones of  Pseudotaxus   land) for his great linguistic support. Furthermore we
            with partly reduced pherophylls present an intermediate   thank Prof. Dr. Th. Stützel (Ruhr-University Bochum,
            link. In Taxaceae it could be shown that the perisporan-  Bochum, Germany) for critical comments that helped to
            giate microsporangiophores of Pseudotaxus, Taxus and   improve the manuscript. We are also grateful to Prof. Dr.
            the terminal synangium of  Cephalotaxus are homolo-  Reinhard Zetter (Department of Palaeontology, Univer-
            gous structures. Accordingly, the perisporangiate micro-  sity of Vienna, Austria) for discussing the pollen mor-
            sporangiophores of Pseudotaxus and Taxus correspond   phology.
            to an entire lateral cone of  Cephalotaxus,  in which all
            lateral hyposporangiate microsporangiophores got re-
            duced. Pollen-cones of  Taxus differ from  Pseudotaxus   5 References
            only in the absence of pherophylls. The hyposporangiate
            microsporangiophores in  Torreya can be regarded as   Bagnell, C. R. 1975: Species distinction among pollen grains of
            derived from a  Taxus-like perisporangiate one. The   Abies,  Picea and  Pinus in the Rocky Mountain Area, a
                                                                  scanning electron microscopy study. Rev. Paleobot. and Pa-
            position and the size correlations indicate that the hypo-
                                                                  lynol. 19: 203–220.
            sporangiate microsporangiophores of  Torreya are ho-
                                                               Bouchal, J. M. 2013: The microflora of the uppermost Eocene
            mologous to microsporangiophores of Taxus and not to   (Priabonian) Florissant Formation, a combined method ap-
            an individual hyposporangiate microsporangiophore of   proach. Diploma University of Vienna.
            Cephalotaxus (e.g. Dörken et al. 2011). Among recent   Callaghan, C. 2011:  Cathaya argyrophylla, some little known
                                                                  facts. Int. Dendrol. Soc. Yearb. 2011: 94–106.
            species of Torreya the number of sporangia per micro-
                                                               Chun, W. Y. & Kuang, K. Z. 1958: A new genus of Pinaceae –
            sporangiophore is not a constant feature and varies   Cathaya Chun et Kuang, gen. nov., from southern and
            strongly, in e.g. T. californica between 4–6 (e.g. Farjon   western China. Bot. Zur. 43: 461–476.
            2010b). Compared to Torreya this variability is quite low   Dallimore, W. & Jackson, A. B. 1966: A Handbook of Coniferae
                                                                                th
            in  Cathaya. Transferring the evolutionary scenario as   and Ginkgoaceae, 4  ed. – Edward Arnold (Publisher) LTD.,
                                                                  London.
            suggested for Taxaceae to Pinaceae, where only hypo-
                                                               Debreczy, Z. &  Racz, I. 2011: Conifers around the world: Coni-
            sporangiate flower-like hyposporangiate pollen-cones   fers of the temperate zones and adjacent regions, Vol. 1. –
            occur, a similar evolutionary pathway could be possible.   DendroPress, Budapest.
            Following the results of developmental studies on pollen-  Den Ouden, P. & Boom, B. K. 1965: Manual of cultivated coni-
            cones in Pinaceae and Taxaceae it could be shown that   fers hardy in the cold- and warm-temperate zone. – Mar-
                                                                  tinus Nijhoff, The Hague, pp. 53–54.
            Pinus  sylvestris and  Picea  sperata on one hand and
                                                               Dluhosch, H. 1937:  Entwicklungsgeschichtliche  Untersuchun-
            Taxus and Torreya on the other hand show great onto-
                                                                  gen über die Mikrosporophylle der Koniferen. Bibl. Bot.
            genetic similarities (Mundry  2000). Mundry’s results   114(3): 1–24.
            indicate that the recent Pinaceae sporangiophores might   Doyle, J. & O’Leary, M. (1935): Pollination in  Pinus. Scient.
            possibly evolved from a Torreya-like ancestor by further   Proc. R.D.S. 21: 181–191.
            reductions of the number of microsporangia per sporan-  Doyle, J. 1945: Developmental lines in Pollination Mechanisms
            giophor. The anomalous microsporangiophores carrying   in the Coniferales. Scient. Proc. R.D.S. 24: 43–62.
            more than two sporangia as developed in Cathaya and   Dörken V. M.; Zhang, Z. X.; Mundry, I. B. & Stützel, Th. 2011:
                                                                  Morphology and anatomy of male reproductive structures
            also in  Picea  asperata (Mundry 2000) might support   in Pseudotaxus chienii (W. C. Cheng) W. C. Cheng (Taxa-
            such an evolutionary scenario, because in these anoma-  ceae). Flora 206(5): 444–450.

            36                                                © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
   7   8   9   10   11   12   13   14